Linde Eckstein SPF 10 Liquid Make-up Recalled for Subpotent Drug Claim
Linde Eckstein is recalling SPF 10 liquid make-up because the sun protection claim cannot be fully guaranteed. The product was distributed throughout the United States.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The FDA classified this recall as Class III, which by definition is unlikely to cause adverse health consequences. The issue is a labeling/efficacy guarantee problem rather than a direct safety hazard like contamination or injury.
Plain-English summary
Linde Eckstein Gmbh + Co KG is recalling Make Up Transparent pastel (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03210. The product is made in Germany and was distributed throughout the United States.
The recall is due to a subpotent drug issue. The products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. The FDA has classified this recall as Class III.
Affected lots include 130917 (Exp 09/13/2017), 310318 (Exp 03/31/2018), 270718 (Exp 07/27/2018), and 081118 (Exp 11/08/2018). Consumers should check their products for these lot numbers and expiration dates.
The recalled product
- Product
- Make Up Transparent pastel (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03210, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 032104.
- Manufacturer
- Linde Eckstein Gmbh + Co KG
- Category
- Drug — OTC Sunscreen
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (8)
- Lot #: 130917
- Exp 09/13/2017
- 310318
- Exp 03/31/2018
- 270718
- Exp 07/27/2018
- 081118
- Exp 11/08/2018.
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 14 recalled by Linde Eckstein Gmbh + Co KG under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 14 products in this recall →Related recalls
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